Участвует в 184 реакциях

3534

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Reaction #2153
7F
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C(=O)Nc1cc2c(O)n(C#CCOC3CCCCO3)cnc-2n1
Reaction #6623
3-(3-tetrahydropyr-2-yloxyprop-1-yn-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
Выход 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)(C)[Si](C)(C)OCC1CC1CCC#CCOC1CCCCO1
Reaction #65088
2-(5-tetrahydropyranyloxy-3-pentynyl)cyclopropylmethyl t-butyldimethylsilyl ether
Выход 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)C1CCC(C#CCOC2CCCCO2)C1
Reaction #65091
3-(tetrahydropyranyloxy-1-propynyl)cyclopentanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)C(=O)C#CCOC1CCCCO1
Reaction #81000
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(C#CCOC1CCCCO1)OCC
Reaction #82210
desired compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)C(=O)C#CCOC1CCCCO1
Reaction #82219
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCCCCCC#CCOC1CCCCO1
Reaction #180682
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC#CCOC1CCCCO1
Reaction #184458
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[SiH](C)OC1(C(O)C#CCOC2CCCCO2)CC(C(C)(C)C)CN1C(=O)OC(C)(C)C
Reaction #208749
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCOC1CCCCO1
Reaction #214232
liquid
Выход 89.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
C[Si](C)(C)C#CCOC1CCCCO1
Reaction #214233
oil
Выход 63.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COC(C(=O)NCc1ccc(C#N)cc1)c1c(F)cccc1C#CCOC1CCCCO1
Reaction #228566
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(CCCC#CCOC1CCCCO1)C(=O)O
Reaction #229407
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C2CCc3cc(OC)ccc3C2(O)C#CCOC2CCCCO2)cc1
Reaction #238795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCOC1CCCCO1
Reaction #265953
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C#CCOC1CCCCO1
Reaction #280403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN1c2sc(C#CCOC3CCCCO3)cc2C(=O)CS1(=O)=O
Reaction #297187
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCC=CCC#CCOC1CCCCO1
Reaction #301182
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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